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32199 publications found in the database

*2016 (534)

*Starting in 2010, coverage has been refocused on core journals.

2016 Publications

Clinical Impact of a Novel MicroRNA Chemo-Sensitivity Predictor in Gastrooesophageal Cancer
Winther, M. et al. Plos One 11(2), NPG, 2016, miRNA Array  PubMed

Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders
Moey, C. et al. European Journal of Human Genetics 24(3), 373-80, 2016  PubMed

Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration
Iqbal, Z. et al. European Journal of Human Genetics 24(3), 392-9, 2016  PubMed

Homozygosity mapping and whole-genome sequencing reveals a deep intronic PROM1 mutation causing cone-rod dystrophy by pseudoexon activation
Mayer, A. K. et al. European Journal of Human Genetics 24(3), 459-62, 2016, CytoScan  PubMed

Long non-coding RNA lnc-MX1-1 is associated with poor clinical features and promotes cellular proliferation and invasiveness in prostate cancer
Jiang, C. Y. et al. Biochemical and Biophysical Research Communications 470(3), 721-7, 2016, Human Gene 2.0 ST Array  PubMed

Biological Characterization of Gene Response to Insulin-Induced Hypoglycemia in Mouse Retina
Emery, M. et al. Plos One 11(2), NPG, 2016, Mouse Gene 1.0 ST array  PubMed

Genome-wide CpG island methylation and intergenic demethylation propensities vary among different tumor sites
Lee, S. T. et al. Nucleic Acids Research 44(3), 1105-17, 2016, Genome-Wide Human SNP Array 6.0  PubMed

An integrated systems biology approach identifies positive cofactor 4 as a factor that increases reprogramming efficiency
Jo, J. et al. Nucleic Acids Research 44(3), 1203-15, 2016  PubMed

Genotype-Specific Interaction of Latent TGFbeta Binding Protein 4 with TGFbeta
Lamar, K. M. et al. Plos One 11(2), NPG, 2016, ExoSAP-IT  PubMed

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